IP Library Granted Patent US 10,617,749
Granted Patent B1
US 10,617,749 · App. 15/441,816 · Granted Apr 14, 2020

Composition of matter and methods for alteration of dendritic cell metabolism to augment cancer vaccine efficacy

Inventors: Brent Hanks (Durham, NC); Fei Zhao (Durham, NC)
Assignee: Duke University
A61K39/0011A61K45/06C12N5/0639A61K2039/5154C12N2501/415C12N2501/72
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Quick Facts
Patent No.
US 10,617,749
App. No.
15/441,816
Granted
Apr 14, 2020
Kind
B1
Abstract

This disclosure provides compositions of matter and methods for alteration of dendritic cell metabolism to augment cancer vaccine efficacy. The compositions and methods can involve regulation of fatty acid oxidation.

Claims (14)

1. A method of treating cancer in a patient treated or being treated with a cancer vaccine, the method comprising:

inhibiting fatty acid oxidation in dendritic cells of the patient.

2. The method of claim 1 , wherein the dendritic cells are ex vivo vaccine-activated dendritic cells and the method further comprises administering a therapeutically effective amount of the ex vivo vaccine-activated dendritic cells to the patient.

3. The method of claim 2 , wherein the method comprises genetically altering the ex vivo vaccine-activated dendritic cells to substantially silence expression of a fatty acid oxidation promoter.

4. The method of claim 3 , wherein the fatty acid oxidation promoter is part of the paracrine Wnt-β-catenin signaling pathway.

5. The method of claim 3 , wherein the fatty acid oxidation promoter is CPT1a, CPT1b, or CPT1c.

6. The method of claim 1 , wherein the dendritic cells are in vivo vaccine-activated dendritic cells and the method comprises administering a therapeutically effective amount of a vector configured to convert native dendritic cells into the in vivo vaccine-activated dendritic cells to the patient.

7. The method of claim 6 , wherein the method comprises administering to the patient a therapeutically effective amount of an inhibitor of a promoter of fatty acid oxidation to inhibit fatty acid oxidation in the in vivo vaccine-activated dendritic cells of the patient.

8. The method of claim 7 , wherein the promoter of fatty acid oxidation in the in vivo vaccine-activated dendritic cells is part of the paracrine Wnt-β-catenin signaling pathway.

9. The method of claim 7 , wherein the promoter of fatty acid oxidation in the in vivo vaccine-activated dendritic cells is CPT1a, CPT1b, or CPT1c.

10. The method of claim 6 , wherein the method comprising administering to the patient a therapeutically effective amount of a transfection or transduction agent configured to transfect or transduce the native dendritic cells or the in vivo vaccine-activated dendritic cells with genetic material that reduces expression of a promoter of fatty acid oxidation.

11. The method of claim 10 , wherein the promoter of fatty acid oxidation is part of the paracrine Wnt-β-catenin signaling pathway.

12. The method of claim 10 , wherein the promoter of fatty acid oxidation is CPT1a, CPT1b, or CPT1c.

13. The method of claim 1 , the method further comprising administering a therapeutically effective amount of a checkpoint inhibitor.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2017
From: HANKS, BRENT; ZHAO, FEI
To: DUKE UNIVERSITY
Reel/Frame 042133/0953 →
Continuity (1)
Provisional Application 62299224 · Feb 24, 2016
Cited By (4)
US 12,220,451 US 12,252,545 US 12,319,925 US 12,599,678